510(k) K926231 ยท HSX Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
DURACON UNICOMPARTMENTAL KNEE SYSTEM
| Applicant | Howmedica Corp., Rutherford NJ, US |
| Decision | Substantially Equivalent, Mar 30, 1993 |
| Received | Dec 11, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926231
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.